Deepthi Yarlagadda

H. Nr: *-**, Sri Pujitha Nilayam,

R.T.C.Colony, Miyapur

Hyderabad-500 049, India

Email:acru2w@r.postjobfree.com

Mobile No: +91-917*******

Career:

Dec 2009 to Present

Sr. Clinical Research Associate

Maya Clinicals, Hyderabad, India

May 2008 – Dec 2009

Clinical Research Associate

Roxaane Research India Pvt Ltd., Chennai, India

Jan 2004 – May 2008

Clinical Research Coordinator

CARE Hospitals, Hyderabad, India

Principal Qualification:

2012

Post Graduate Diploma In Clinical Research and Regulatory Affairs from Sikkim Manipal University, India

May 2002

Bachelor of Sciences in Chemistry, Physics and Mathematics from Kakatiya University, Warangal, India

2000

Diploma in Computer Applications

Participation in training Programs:

Apr 2008

Human Participants Protection Education For Research Teams online course, Sponsored by the National Institutes of Health(NIH), USA

Feb 2006

Clinical Excellence Program Organised by SIRO Clinpharma Pvt., Ltd., Hyderabad, India

Feb 2006

GCP Training as part of Investigator Meeting Organised by Pfizer Pharma Ltd, Hyderabad, India

Jul 2006

GCP Training as part of Investigator Meeting organised by Aventis Pharma Ltd., Bangalore, India

Project Experience:

Indication

Position

Phase

Prostate Cancer

Sr. CRA

III

Colorectal Cancer

Sr. CRA

III

Pancreatic Cancer

Sr. CRA

III

Chron’s Disease

Sr. CRA

IIb/III

Multiple Sclerosis

Sr. CRA

III

Melanoma

CRA

III

Asthma Study

CRA

III

RA

CRA

III

Neurology

CRA

III

MI

Sr.CRC

III

MI

Sr.CRC

III

AF

Sr.CRC

III

MI

CRC

III

PTCA Registry

CRC

Registry

Competencies in clinical trials:

My experience in conducting clinical trials has been acquired from several angles

Adept in managing the wide spectrum of tasks including site and investigator selection, initiation, monitoring, training & guiding CRAs/CRCs and Investigational site staff, administrative and team management.

Been involved in writing and reviewing of various SOPs, Project Specific Guidelines and Forms.

Working experience with higher management to ensure proper planning, execution.

Well versed in preparing, and execution of site budgets, contracts and negotiations.

Regulatory Dossier submissions & approvals (IRB & DCGI)

Well organised Investigator Meetings

Logistics and study supplies management

Proven studies in Recruitment Strategies

Project Management

Team training and motivation

Well expertise preparing study update/reporting trackers in excel environment.

Achievements:

Handled more than 200 trial feasibilities in all major therapeutic areas.

Conducted more than 9 international clinical trials right from feasibility to close-out.

Independently identified sites across India that was well qualified by global sponsors.

Recruitment strategies that implemented to recruit end number of patients.

Successfully processed several applications to DCGI and received approvals.

Personal Strengths:

Focused, structured and quality minded

Strong team player, but enjoy working independently as well

Strong at planning, coordinating and reaching consensus

Thorough, efficient, flexible and conscientious

Adapt easily to a changing environment with tight deadlines

Extrovert with a positive can do attitude

Languages:

English: Excellent

Telugu: Mother tongue

Hindi: Good at Speak, Read and Write

Tamil: Knowledge and understand

Skills:

Microsoft office (Word, Excel, Power point, Outlook)

Electronic Data Capture – Inform, Oracle,

IVRS/IWRS – CliniPhone

Personal Profile:

Date of Birth : 07 Aug 1981

Marital Status : Married

Nationality : Indian

Hobbies : Reading Books and Music

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